1. Lopez-Escamez, Jose A, Liu, Ying. 2023. Epidemiology and genetics of Meniere's disease. In Current opinion in neurology, 37, 88-94. doi:10.1097/WCO.0000000000001227. https://pubmed.ncbi.nlm.nih.gov/37865853/
2. Karali, Marianthi, Testa, Francesco, Di Iorio, Valentina, Simonelli, Francesca, Banfi, Sandro. 2022. Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in Italy. In Scientific reports, 12, 20815. doi:10.1038/s41598-022-24636-1. https://pubmed.ncbi.nlm.nih.gov/36460718/
3. Lopes, Vanda S, Williams, David S. 2015. Gene Therapy for the Retinal Degeneration of Usher Syndrome Caused by Mutations in MYO7A. In Cold Spring Harbor perspectives in medicine, 5, . doi:10.1101/cshperspect.a017319. https://pubmed.ncbi.nlm.nih.gov/25605753/
4. Gilmore, W Blake, Hultgren, Nan W, Chadha, Abhishek, Canto-Soler, M Valeria, Williams, David S. 2023. Expression of two major isoforms of MYO7A in the retina: Considerations for gene therapy of Usher syndrome type 1B. In Vision research, 212, 108311. doi:10.1016/j.visres.2023.108311. https://pubmed.ncbi.nlm.nih.gov/37586294/
5. Schott, Juliane W, Huang, Peixin, Morgan, Michael, Schambach, Axel, Staecker, Hinrich. 2023. Third-generation lentiviral gene therapy rescues function in a mouse model of Usher 1B. In Molecular therapy : the journal of the American Society of Gene Therapy, 31, 3502-3519. doi:10.1016/j.ymthe.2023.10.018. https://pubmed.ncbi.nlm.nih.gov/37915173/
6. Lu, Ye, Zhou, Diana, King, Rebecca, Geisert, Eldon E, Lu, Lu. 2018. The genetic dissection of Myo7a gene expression in the retinas of BXD mice. In Molecular vision, 24, 115-126. doi:. https://pubmed.ncbi.nlm.nih.gov/29430167/
7. Fuster-García, Carla, García-Bohórquez, Belén, Rodríguez-Muñoz, Ana, Millán, José M, García-García, Gema. 2021. Usher Syndrome: Genetics of a Human Ciliopathy. In International journal of molecular sciences, 22, . doi:10.3390/ijms22136723. https://pubmed.ncbi.nlm.nih.gov/34201633/
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